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NEET CHEMISTRYAlcohols, Phenols and EthersMedium

Question

Among the following, which hydrolysis reaction occurs at the slowest rate:

A

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B

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C

4

D

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Step-by-Step Solution

The rate of hydrolysis (nucleophilic substitution) depends heavily on the nature of the carbon-halogen bond. Aryl halides and vinyl halides are extremely unreactive towards hydrolysis because the lone pair of electrons on the halogen atom is in conjugation with the π\pi-electrons of the benzene ring or double bond. This resonance imparts a partial double bond character to the C-X bond, making it very difficult to break. In contrast, standard alkyl, allylic, and benzylic halides undergo hydrolysis much more readily via SN1S_N1 or SN2S_N2 mechanisms. Since the structural options are missing from the provided text, the exact correct option cannot be visually evaluated and verified.

Exam Context & Concepts Covered

This question aligns with the NEET CHEMISTRY syllabus, specifically targeting concepts from Alcohols, Phenols and Ethers. Mastering this topic is crucial for scoring well in the upcoming medical entrance examinations. Solving conceptually related problems will help you understand the nuances of these concepts and improve your problem-solving speed.

CHEMISTRYAlcohols, Phenols and Ethersfollowinghydrolysisreactionoccursslowest

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